OPA1 mutations impair mitochondrial function in both pure and complicated dominant optic atrophy

被引：30
|
作者：
Yu-Wai-Man, Patrick [1 ,2 ,3 ]
Trenell, Michael I. [4 ]
Hollingsworth, Kieren G. [4 ]
Griffiths, Philip G. [2 ,3 ]
Chinnery, Patrick F. [1 ,2 ]
机构：
[1] Newcastle Univ, Inst Human Genet, Newcastle Upon Tyne NE1 3BZ, Tyne & Wear, England
[2] Newcastle Univ, Mitochondrial Res Grp, Inst Ageing & Hlth, Sch Med, Newcastle Upon Tyne NE1 3BZ, Tyne & Wear, England
[3] Royal Victoria Infirm, Dept Ophthalmol, Newcastle Upon Tyne NE1 4LP, Tyne & Wear, England
[4] Newcastle Univ, Newcastle Magnet Resonance Ctr, Inst Ageing & Hlth, Newcastle Upon Tyne NE1 3BZ, Tyne & Wear, England
来源：
BRAIN | 2011年 / 134卷
基金：
英国惠康基金; 英国医学研究理事会;
关键词：
MAGNETIC-RESONANCE-SPECTROSCOPY; IN-VIVO; NEUROPATHY; DISEASE;
D O I：
10.1093/brain/awq288
中图分类号：
R74 [神经病学与精神病学];
学科分类号：
摘要：
引用
收藏
页数：5
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